BOBBI BROWN TINTED MOISTURIZER BROAD SPECTRUM SPF 15

Manufacturer
Bobbi Brown Professional Cosmetics Inc. | Estee Lauder Companies Inc. | Estee Lauder N.V.
Effective date
2024-12-07
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 20:46:51

Label at a glance#

ProductBOBBI BROWN TINTED MOISTURIZER BROAD SPECTRUM SPF 15
Active ingredientOCTINOXATE, TITANIUM DIOXIDE
Label structure9 sections

Dosage and administration

For sunscreen use: apply liberally 15 minutes before sun exposure reapply at least every two hours use a water resistant sunscreen if swimming or sweating Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in...

Storage and handling

Protect the product in this container from excessive heat and direct sun.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7.50%

Titanium Dioxide 3.00%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

Helps prevent sunburn

Warnings

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

For sunscreen use:

  • apply liberally 15 minutes before sun exposure
  • reapply at least every two hours
  • use a water resistant sunscreen if swimming or sweating
  • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
    • limit time in the sun, especially from 10 a.m.–2 p.m.
    • wear long-sleeved shirts, pants, hats and sunglasses
  • children under 6 months of age: ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

water\aqua\eau • phenyl trimethicone • butylene glycol • pentaerythrityl tetraoctanoate • simmondsia chinensis (jojoba) seed oil • petrolatum • biosaccharide gum - 1 • steareth-21 • glyceryl stearate • sodium hyaluronate • tocopheryl acetate • polymethyl methacrylate • magnesium aluminum silicate • ethylhexylglycerin • caprylyl glycol • cetyl alcohol • acrylamide/sodium acryloyldimethyltaurate copolymer • peg-12 dimethicone • isohexadecane • lecithin • xanthan gum • steareth-2 • potassium stearate • citric acid • fragrance (parfum) • limonene • linalool • benzyl salicylate • polysorbate 80 • disodium edta • phenoxyethanol • sorbic acid • [+/- titanium dioxide (ci 77891) • iron oxides (ci 77491, ci 77492, ci 77499)] <iln33789>

Other information

STORAGE AND HANDLING SECTION

Protect the product in this container from excessive heat and direct sun.

PRINCIPAL DISPLAY PANEL - 50 ml Tube Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SPF 15

Tinted

Moisturizer

Broad

Spectrum

SPF 15

BOBBI BROWN

1.7 FL. OZ./50 ml e

Principal Display PanelPrincipal Display Panel

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64141-027BOBBI BROWN TINTED MOISTURIZER BROAD SPECTRUM SPF 15 (OCTINOXATE AND TITANIUM DIOXIDE) LOTION [BOBBI BROWN PROFESSIONAL COSMETICS INC.]8Legacy NDC20241213_7c8d3d8f-2ba0-40df-a972-51c9269f210b.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 34 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64141-02764141-027-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 32 matching rows.

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
38e566b7-9250-2731-e063-6294a90ad2637c8d3d8f-2ba0-40df-a972-51c9269f210b2025-06-30WarningsExact identifier
spl set id: 7c8d3d8f-2ba0-40df-a972-51c9269f210b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.